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724179008: Laron syndrome with immunodeficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3431583010 Laron syndrome with immunodeficiency (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3431584016 Laron syndrome with immunodeficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3431585015 Laron-like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3431586019 Short stature due to STAT5b (signal transducer and activator of transcription 5b) deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5403271016 This syndrome is characterized by severe growth retardation associated with immunodeficiency. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403272011 This syndrome is characterised by severe growth retardation associated with immunodeficiency. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3431583010 Laron syndrome with immunodeficiency (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3431584016 Laron syndrome with immunodeficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3431585015 Laron-like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3431586019 Short stature due to STAT5b (signal transducer and activator of transcription 5b) deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3431587011 This syndrome has characteristics of severe growth retardation associated with immunodeficiency. Less than 10 cases have been described in literature. Individuals present with typical clinical and biochemical features of Laron syndrome such as post-natal growth retardation, delayed bone age and facial dysmorphism (prominent forehead, hypoplastic nasal bridge), and low serum IGF-1 concentrations with normal or high GH concentrations. Immunodeficiency has manifestations of moderate lymphopenia which leads to recurrent infections of the skin and respiratory tract. The syndrome is due to mutation in the signal transducer and activator of transcription 5b gene (STAT5b). Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403271016 This syndrome is characterized by severe growth retardation associated with immunodeficiency. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403272011 This syndrome is characterised by severe growth retardation associated with immunodeficiency. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3445231001000114 Laron-Syndrom mit Immundefekt de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
956361000172114 syndrome de Laron avec déficit immunitaire fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
974281000172115 petite taille par déficit en Stat5b fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
956361000172114 syndrome de Laron avec déficit immunitaire fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
974281000172115 petite taille par déficit en Stat5b fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3445231001000114 Laron-Syndrom mit Immundefekt de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Laron syndrome with immunodeficiency (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Laron syndrome with immunodeficiency (disorder) Is a Short stature disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Laron syndrome with immunodeficiency (disorder) Is a Combined immunodeficiency disease true Inferred relationship Existential restriction modifier (core metadata concept)
Laron syndrome with immunodeficiency (disorder) Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier (core metadata concept)
Laron syndrome with immunodeficiency (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Laron syndrome with immunodeficiency (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Laron syndrome with immunodeficiency (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Laron syndrome with immunodeficiency (disorder) Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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